Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31)
<p>Abstract</p> <p>Background</p> <p>Mutations in the <it>SPG4 </it>gene (spastin) and in the <it>SPG3A </it>gene (atlastin) account for the majority of 'pure' autosomal dominant form of hereditary spastic paraplegia (HSP). Recently, mu...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2008-07-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |